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临床试验/NCT07319689
NCT07319689已完成不适用

Predictors of Myasthenia Gravis Outcome Following Thoracoscopic Thymectomy: Multicenter Comparative Study Between Thymomatous and Non-Thymomatous Patients

Tanta University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
Proportion of patients achieving complete stable remission

研究概览

简要总结

This study aimed to assess and compare predictors of outcome in patients with thymomatous and non-thymomatous MG undergoing Thoracoscopic thymectomy.

详细描述

Myasthenia Gravis (MG) is a chronic autoimmune neuromuscular disorder characterized by fluctuating muscle weakness resulting from antibodies that target acetylcholine receptors or associated proteins at the neuromuscular junction.

Thoracoscopic thymectomy becomes more prominent than traditional transsternal thymectomy due to fewer perioperative complications with shorter hospital stays and more favorable long-term outcomes.

Prognostic outcomes following thoracoscopic thymectomy can vary significantly between non-thymomatous and thymomatous MG, necessitating a thorough investigation of these differences.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Both sexes.
  • Confirmed diagnosis of Myasthenia Gravis (MG).
  • Underwent Thoracoscopic thymectomy.
  • Availability of complete preoperative and postoperative records, including imaging and histopathology.
  • Minimum follow-up of 9 months post-surgery.

排除标准

  • Patients who underwent thymectomy for indications other than MG.
  • Incomplete medical records or loss to follow-up before outcome assessment.
  • Patients with concomitant neuromuscular disorders other than MG

研究组 & 干预措施

Thymomatous Myasthenia Gravis group

Thymomatous myasthenia gravis (patients with histologically confirmed thymoma).

干预措施: Data collection (Other)

Non-thymomatous Myasthenia Gravis group

Non-thymomatous myasthenia gravis (patients with thymic hyperplasia or normal/ involuted thymus).

干预措施: Data collection (Other)

结局指标

主要结局

Proportion of patients achieving complete stable remission

时间窗: 12 months post-procedure

Proportion of patients achieving complete stable remission was recorded.

次要结局

  • Proportion of patients achieving pharmacologic remission(12 months post-procedure)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mostafa Mohamed Elawady

Lecturer of Neuropsychiatry, Tanta University, Tanta, Egypt.

Tanta University

研究点 (1)

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